Waterman-Storer C M, Karki S, Holzbaur E L
Department of Animal Biology, University of Pennsylvania School of Veterinary Medicine, Philadelphia 19104-6046.
Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1634-8. doi: 10.1073/pnas.92.5.1634.
p150Glued was first identified as a polypeptide that copurifies with cytoplasmic dynein, the minus-end-directed microtubule-based motor protein, and has more recently been shown to be present as a member of the oligomeric dynactin complex, which includes the actin-related protein centractin (Arp-1). Dynactin is thought to mediate dynein-driven vesicle motility, as well as nuclear transport, in lower eukaryotes. The mechanism by which dynactin may function in these cellular processes is unknown. To examine the role of the dynactin complex in vivo, we overexpressed the rat cDNA encoding p150Glued in Rat-2 fibroblasts. Overexpression of full-length, as well as C-terminal deletion, constructs resulted in the decoration of microtubules with the p150Glued polypeptides. This cellular evidence for microtubule association was corroborated by in vitro microtubule-binding assays. Amino acids 39-150 of p150Glued were determined to be sufficient for microtubule association. We also tested for a direct interaction between p150Glued and centractin. In vitro translated centractin was specifically retained by a p150Glued affinity column, and this interaction was blocked by a synthetic peptide which corresponds to a highly conserved motif from the C terminus of p150Glued. These results demonstrate that p150Glued, a protein implicated in cytoplasmic dynein-based microtubule motility, is capable of direct binding to both microtubules and centractin.
p150Glued最初被鉴定为一种与胞质动力蛋白共纯化的多肽,胞质动力蛋白是一种基于微管的负端定向运动蛋白,最近被证明是寡聚动力蛋白复合体的成员之一,该复合体包括肌动蛋白相关蛋白centractin(Arp-1)。在低等真核生物中,动力蛋白被认为介导动力蛋白驱动的囊泡运动以及核运输。动力蛋白在这些细胞过程中发挥作用的机制尚不清楚。为了研究动力蛋白复合体在体内的作用,我们在大鼠-2成纤维细胞中过表达了编码p150Glued的大鼠cDNA。全长以及C端缺失构建体的过表达导致微管被p150Glued多肽修饰。体外微管结合试验证实了这种微管结合的细胞证据。确定p150Glued的39-150位氨基酸足以与微管结合。我们还测试了p150Glued与centractin之间的直接相互作用。体外翻译的centractin被p150Glued亲和柱特异性保留,并且这种相互作用被一种合成肽阻断,该合成肽对应于p150Glued C端的一个高度保守基序。这些结果表明,p150Glued这种与基于胞质动力蛋白的微管运动有关的蛋白质,能够直接与微管和centractin结合。